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This involves the development of a control system architecture, selecting the components to be used, detailing schematic diagrams and system documentation, programming controllers (PLC, DCS, RTU), programming the process visualization (HMI/SCADA), developing databases for archiving/displaying historical system data and implementing/commissioning the control system at the client’s facility.
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Familiarity with firmware and digital control - DSP, FPGA. Experience with designing and testing complex power supply circuity - PFC, Inverters, Battery Chargers, Power Supplies, Control Circuits.
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We are seeking a quality control professional from the chemicals, pharmaceutical, or biotech industries to assist in the analysis and verification of a range of flow battery electrolyte samples.
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Coordinate with key committees and medical management structures including but not limited to Hospital Leadership, DPH Chief Nursing Officer, infection control, pharmacy, medical records, quality improvement, and other required hospital committees.
$88,182.79 - $135,742.36 a yearFull-timeExpandApply NowActive JobUpdated 15 days ago - UpvoteDownvoteShare Job
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Experience using basic social economic and social psychology research and study design and administration processes from the planning and formulation of concepts through specification and analysis of output to the presentation of conclusions and control of the studies.
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Perform work that is compliant with cGMP, ISO, QMS and other pertinent regulations and directives. The Production Operator will be a highly skilled production operator which will include ensuring that we meet the demand for products, production quality levels and production yield goals while maintaining cost control.
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Experience using scripting languages (Python, etc) to control hardware resources like LabJack, Arduino, or Raspberry Pi. Fikst has a growing embedded systems team, focusing on providing microcontroller and embedded firmware solutions for electromechanical control across a wide variety of technologies and industries.
Full-timeExpandApply NowActive JobUpdated 23 days ago - UpvoteDownvoteShare Job
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Minimum of 1 - 3 years experience in Quality Assurance and Quality Control of Drug Products, Good Manufacturing Practice (cGMP) and FDA inspection, manufacturing, or quality unit. Develops and manages the QA and QC system in a regulated radiopharmaceutical environment with regards to U.S. FDA cGMP and international regulations.
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Applicants must be either a U.S. citizen, U.S. national, legal permanent resident, asylee, refugee or must be eligible to apply for and obtain the appropriate export control license from the U.S. Departments of State or Commerce.
$140,000 - $195,000 a yearFull-timeExpandApply NowActive JobUpdated 22 days ago - UpvoteDownvoteShare Job
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Review and approve supplier deviations, change control, CAPA, and OOS investigations. Minimum of 7-10 years quality assurance / supplier quality engineering experience in a pharmaceutical/life-science environment.
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This Opportunity allows for a lot of growth and ability to work with QC Chemistry practices!
$50,000 - $60,000 a yearFull-timeExpandApply NowActive JobUpdated 22 days ago - UpvoteDownvoteShare Job
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Work with Quality Control to resolve supplier quality issues. Experience with plastics processing (extrusion, injection molding, fiber forming) is a plus. Lead efforts to address non-conformances through the NCR/CAPA system - driving escalation when risk level warrants it.
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Job Preferences: 1-3 years prior experience on servicing thermal imaging equipment is a plus Soldering, assembly, and troubleshooting of electrical systems Good SAP experience Applicants must be either a U.S. citizen, U.S. national, legal permanent resident, asylee, refugee or must be eligible to apply for and obtain the appropriate export control license from the U.S. Departments of State or Commerce.
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Follows company and industry standards outlined in procedural and quality policies Properly implements drawing changes and creates drawings in accordance with applicable ASME Y14 standards Supports the Document Control Function by vaulting documents into the PLM system.
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Experience working with electronic document systems ( CMMS work orders ,LMS, Track Wise, Master Control ) or similar systems. Support pharmaceutical manufacturing plant, equipment, and utilities, and maintain compliance with all state and federal guidelines with emphasis on current Good Manufacturing Practices (cGMP) and Good Documentation Practices (cGDP) requirements.
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cgmp control jobs Company: Randstad Usa in Lowell, MA
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